Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 29 c.3671C>A r.(?) p.(Ala1224Asp) - Paternal (confirmed) - pathogenic (recessive) g.76901105C>A - c.3671C>A - MYO7A_001060 - PubMed: Ma 2016 - - Germline yes 0/120 healthy controls - - - DNA SEQ-NG, SEQ blood - retinal disease II:1 PubMed: Ma 2016 sister of II:2 F - China chinese - - - - 1 LOVD
+/. 29 c.3671C>A r.(?) p.(Ala1224Asp) - Paternal (confirmed) - pathogenic (recessive) g.76901105C>A - c.3671C>A - MYO7A_001060 - PubMed: Ma 2016 - - Germline yes 0/120 healthy controls - - - DNA SEQ-NG, SEQ blood - retinal disease II:2 PubMed: Ma 2016 brother of II:1 M - China chinese - - - - 1 LOVD
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